ClinVar Miner

Submissions for variant NM_152743.4(BRAT1):c.1230T>C (p.Ser410=) (rs1583301772)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000938000 SCV001083795 likely benign not provided 2018-05-30 criteria provided, single submitter clinical testing
Invitae RCV001452951 SCV001656631 likely benign Rigidity and multifocal seizure syndrome, lethal neonatal 2018-05-14 criteria provided, single submitter clinical testing

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